Incidental Mutation 'IGL03391:Serpinb3a'
| ID |
421049 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Serpinb3a
|
| Ensembl Gene |
ENSMUSG00000044594 |
| Gene Name |
serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3A |
| Synonyms |
Sqn5 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.059)
|
| Stock # |
IGL03391
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
1 |
| Chromosomal Location |
106973317-106980033 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 106974072 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 280
(S280P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000108337
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027567]
[ENSMUST00000112717]
|
| AlphaFold |
G3X9V8 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000027567
AA Change: S280P
PolyPhen 2
Score 0.806 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000027567
Gene: ENSMUSG00000044594
AA Change: S280P
| Domain | Start | End | E-Value | Type |
|---|
|
SERPIN
|
13 |
387 |
6.36e-182 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000112717
AA Change: S280P
PolyPhen 2
Score 0.806 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000108337
Gene: ENSMUSG00000044594
AA Change: S280P
| Domain | Start | End | E-Value | Type |
|---|
|
SERPIN
|
13 |
387 |
6.36e-182 |
SMART |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the serpin family of serine protease inhibitors. The encoded protein is highly expressed in many tumor cells and can inactivate granzyme M, an enzyme that kills tumor cells. This protein, along with serpin B3, can be processed into smaller fragments that aggregate to form an autoantigen in psoriasis, probably by causing chronic inflammation. [provided by RefSeq, Jan 2017]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced susceptibility to allergen-induced airway hyperresponsiveness. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca14 |
A |
G |
7: 119,846,107 (GRCm39) |
D586G |
probably damaging |
Het |
| Acadvl |
A |
C |
11: 69,901,542 (GRCm39) |
M557R |
probably damaging |
Het |
| Ano2 |
T |
A |
6: 125,784,802 (GRCm39) |
N327K |
probably damaging |
Het |
| Cdh11 |
A |
T |
8: 103,400,655 (GRCm39) |
D104E |
possibly damaging |
Het |
| Chrnb2 |
A |
G |
3: 89,668,184 (GRCm39) |
F377S |
probably damaging |
Het |
| Cngb1 |
T |
C |
8: 96,030,333 (GRCm39) |
|
probably benign |
Het |
| Dnaaf1 |
C |
T |
8: 120,309,355 (GRCm39) |
R148C |
probably damaging |
Het |
| Esrrg |
A |
T |
1: 187,882,420 (GRCm39) |
I226F |
possibly damaging |
Het |
| Evl |
C |
A |
12: 108,642,358 (GRCm39) |
|
probably null |
Het |
| Gpam |
T |
C |
19: 55,070,128 (GRCm39) |
E376G |
probably damaging |
Het |
| Gzf1 |
C |
A |
2: 148,525,603 (GRCm39) |
R25S |
probably damaging |
Het |
| Ighv5-2 |
A |
T |
12: 113,542,138 (GRCm39) |
Y113* |
probably null |
Het |
| Izumo4 |
A |
G |
10: 80,540,947 (GRCm39) |
T216A |
probably damaging |
Het |
| Lrp1b |
T |
G |
2: 41,185,653 (GRCm39) |
Y1354S |
possibly damaging |
Het |
| Mark1 |
A |
G |
1: 184,651,632 (GRCm39) |
|
probably benign |
Het |
| Mylpf |
A |
G |
7: 126,812,349 (GRCm39) |
I17V |
probably benign |
Het |
| Myo18b |
C |
A |
5: 113,022,345 (GRCm39) |
|
probably benign |
Het |
| Nbas |
C |
T |
12: 13,533,750 (GRCm39) |
A1795V |
probably benign |
Het |
| Oprm1 |
A |
C |
10: 6,964,077 (GRCm39) |
|
probably benign |
Het |
| Or2ag15 |
A |
T |
7: 106,340,962 (GRCm39) |
Y60N |
probably damaging |
Het |
| Or5b122 |
A |
G |
19: 13,563,483 (GRCm39) |
M272V |
probably benign |
Het |
| Or5w1 |
A |
G |
2: 87,487,032 (GRCm39) |
S78P |
possibly damaging |
Het |
| Parp14 |
T |
C |
16: 35,678,640 (GRCm39) |
M443V |
probably benign |
Het |
| Psca |
T |
C |
15: 74,586,717 (GRCm39) |
F5S |
probably benign |
Het |
| Ptbp2 |
A |
T |
3: 119,514,031 (GRCm39) |
Y514* |
probably null |
Het |
| Scg3 |
A |
G |
9: 75,568,533 (GRCm39) |
|
probably null |
Het |
| Scn2a |
T |
C |
2: 65,594,557 (GRCm39) |
V1802A |
probably damaging |
Het |
| Slc39a14 |
T |
C |
14: 70,547,291 (GRCm39) |
I352V |
probably damaging |
Het |
| Slc6a2 |
G |
T |
8: 93,688,080 (GRCm39) |
V69L |
probably damaging |
Het |
| Slc8a1 |
A |
G |
17: 81,740,067 (GRCm39) |
|
probably benign |
Het |
| Tjp1 |
T |
C |
7: 64,964,717 (GRCm39) |
D818G |
probably damaging |
Het |
| Tnfaip8 |
T |
C |
18: 50,223,552 (GRCm39) |
V120A |
probably damaging |
Het |
| Trmt5 |
G |
A |
12: 73,328,226 (GRCm39) |
H326Y |
probably benign |
Het |
| Vmn1r222 |
T |
C |
13: 23,416,632 (GRCm39) |
M194V |
possibly damaging |
Het |
| Zbtb17 |
A |
G |
4: 141,194,069 (GRCm39) |
E699G |
probably damaging |
Het |
|
| Other mutations in Serpinb3a |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01113:Serpinb3a
|
APN |
1 |
106,978,789 (GRCm39) |
nonsense |
probably null |
|
|
IGL01940:Serpinb3a
|
APN |
1 |
106,973,915 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02077:Serpinb3a
|
APN |
1 |
106,974,111 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02136:Serpinb3a
|
APN |
1 |
106,974,015 (GRCm39) |
missense |
probably benign |
0.15 |
|
IGL02214:Serpinb3a
|
APN |
1 |
106,976,218 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02239:Serpinb3a
|
APN |
1 |
106,979,418 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02508:Serpinb3a
|
APN |
1 |
106,973,802 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02533:Serpinb3a
|
APN |
1 |
106,974,892 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02860:Serpinb3a
|
APN |
1 |
106,977,183 (GRCm39) |
splice site |
probably benign |
|
|
IGL03013:Serpinb3a
|
APN |
1 |
106,973,813 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0321:Serpinb3a
|
UTSW |
1 |
106,975,212 (GRCm39) |
nonsense |
probably null |
|
|
R0416:Serpinb3a
|
UTSW |
1 |
106,977,116 (GRCm39) |
missense |
probably benign |
0.29 |
|
R0494:Serpinb3a
|
UTSW |
1 |
106,975,212 (GRCm39) |
nonsense |
probably null |
|
|
R0498:Serpinb3a
|
UTSW |
1 |
106,974,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1223:Serpinb3a
|
UTSW |
1 |
106,975,282 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1596:Serpinb3a
|
UTSW |
1 |
106,974,904 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1655:Serpinb3a
|
UTSW |
1 |
106,973,942 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2156:Serpinb3a
|
UTSW |
1 |
106,975,202 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2296:Serpinb3a
|
UTSW |
1 |
106,975,291 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4327:Serpinb3a
|
UTSW |
1 |
106,979,500 (GRCm39) |
start codon destroyed |
probably damaging |
1.00 |
|
R4612:Serpinb3a
|
UTSW |
1 |
106,975,337 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4830:Serpinb3a
|
UTSW |
1 |
106,976,316 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5016:Serpinb3a
|
UTSW |
1 |
106,974,060 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5483:Serpinb3a
|
UTSW |
1 |
106,974,899 (GRCm39) |
missense |
probably benign |
0.16 |
|
R5619:Serpinb3a
|
UTSW |
1 |
106,974,838 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7227:Serpinb3a
|
UTSW |
1 |
106,979,359 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8277:Serpinb3a
|
UTSW |
1 |
106,973,970 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8526:Serpinb3a
|
UTSW |
1 |
106,976,504 (GRCm39) |
splice site |
probably null |
|
|
R8992:Serpinb3a
|
UTSW |
1 |
106,974,907 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9335:Serpinb3a
|
UTSW |
1 |
106,974,886 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9799:Serpinb3a
|
UTSW |
1 |
106,974,892 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1177:Serpinb3a
|
UTSW |
1 |
106,978,738 (GRCm39) |
critical splice donor site |
probably null |
|
|
| Posted On |
2016-08-02 |
Incidental Mutation